Canonical Allele Identifier: CA2654931558

Gene: SLC19A1

Linked Data

• gnomAD v4: 21-45544397-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.45544397A>G , CM000683.2:g.45544397A>G	GRCh38
NC_000021.8:g.46964311A>G , CM000683.1:g.46964311A>G	GRCh37
NC_000021.7:g.45788739A>G	NCBI36
NG_028278.1:g.3075T>C
NG_028278.2:g.23747T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650808.1:c.-49-6389T>C	ENSP00000498221.1:n.-49-6389T>C
ENST00000443742.1:c.-310T>C	ENSP00000411345.1:n.-310T>C
ENST00000528477.1:c.-393T>C	ENSP00000435780.1:n.-393T>C
ENST00000567670.5:c.-310T>C	ENSP00000457278.1:n.-310T>C
XM_011529696.1:c.33-51T>C	XP_011527998.1:n.33-51T>C
XM_011529697.1:c.33-51T>C	XP_011527999.1:n.33-51T>C
XM_011529700.1:c.-49-6389T>C	XP_011528002.1:n.-49-6389T>C
XM_011529701.1:c.-393T>C	XP_011528003.1:n.-393T>C
XM_011529705.1:c.33-51T>C	XP_011528007.1:n.33-51T>C
XM_011529707.1:c.33-51T>C	XP_011528009.1:n.33-51T>C
XM_011529708.1:c.-254-56T>C	XP_011528010.1:n.-254-56T>C
XM_011529709.1:c.-407-6389T>C	XP_011528011.1:n.-407-6389T>C
XM_011529710.1:c.-165-12249T>C	XP_011528012.1:n.-165-12249T>C
NM_001352511.1:c.-49-6389T>C	NP_001339440.1:n.-49-6389T>C
XM_011529696.2:c.33-51T>C	XP_011527998.1:n.33-51T>C
XM_011529700.2:c.-49-6389T>C	XP_011528002.1:n.-49-6389T>C
XM_011529701.2:c.-393T>C	XP_011528003.1:n.-393T>C
XM_011529709.2:c.-407-6389T>C	XP_011528011.1:n.-407-6389T>C
XM_017028444.1:c.33-51T>C	XP_016883933.1:n.33-51T>C
XM_017028445.2:c.33-51T>C	XP_016883934.1:n.33-51T>C
NM_001352511.2:c.-49-6389T>C	NP_001339440.1:n.-49-6389T>C
NM_001352511.3:c.-49-6389T>C	NP_001339440.1:n.-49-6389T>C